{{Rsnum
|rsid=111033348
|Chromosome=7
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC26A4
|position=107674326
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC26A4
}}{{omim
|id=605646
|rsnum=111033348
|variant=0019
}}{{ClinVar
|rsid=111033348
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=107314771
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=SLC26A4:5172
|GENE_NAME=SLC26A4
|GENE_ID=5172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.107314771C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605646.0019
|CLNSIG=5
|CLNCUI=C0271829
|CLNDBN=Pendred's syndrome; Hereditary hearing loss and deafness
|Disease=Pendred's syndrome; Hereditary hearing loss and deafness
|CLNACC=RCV000005101.1; RCV000036499.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:NBK1467:C0271829:274600:705:70348004; NBK1434:C0236038:95827002
}}{{PMID Auto
|PMID=10878664
|Title=Deafness heterogeneity in a Druze isolate from the Middle East: novel OTOF and PDS mutations, low prevalence of GJB2 35delG mutation and indication for a new DFNB locus.
}}

{{PMID Auto
|PMID=15355436
|Title=Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.
}}